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First published online June 22, 2006
doi: 10.1242/10.1242/dev.02439
1 Max Planck Institute of Molecular Cell Biology and Genetics,
Pfotenhauerstr.108, 01307 Dresden, Germany.
2 Instituto de Medicina Molecular, Edificio Egas Moniz, Av. Profesor Egas Moniz,
1649-028 Lisbon, Portugal.
* Author for correspondence (e-mail: heisenberg{at}mpi-cbg.de)
Accepted 9 May 2006
Epithelial morphogenesis depends on coordinated changes in cell shape, a process that is still poorly understood. During zebrafish epiboly and Drosophila dorsal closure, cell-shape changes at the epithelial margin are of critical importance. Here evidence is provided for a conserved mechanism of local actin and myosin 2 recruitment during theses events. It was found that during epiboly of the zebrafish embryo, the movement of the outer epithelium (enveloping layer) over the yolk cell surface involves the constriction of marginal cells. This process depends on the recruitment of actin and myosin 2 within the yolk cytoplasm along the margin of the enveloping layer. Actin and myosin 2 recruitment within the yolk cytoplasm requires the Ste20-like kinase Msn1, an orthologue of Drosophila Misshapen. Similarly, in Drosophila, actin and myosin 2 localization and cell constriction at the margin of the epidermis mediate dorsal closure and are controlled by Misshapen. Thus, this study has characterized a conserved mechanism underlying coordinated cell-shape changes during epithelial morphogenesis.
Key words: Zebrafish epiboly, Drosophila dorsal closure, Cell shape, Misshapen, Actin, Myosin 2
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